Canonical Allele Identifier: CA265633064

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91969962_91969965dup , CM000676.2:g.91969962_91969965dup	GRCh38
NC_000014.8:g.92436306_92436309dup , CM000676.1:g.92436306_92436309dup	GRCh37
NC_000014.7:g.91506059_91506062dup	NCBI36
NG_016970.1:g.75095_75098dup

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.5720-72_5720-69dup MANE Select	NP_004230.2:n.5720-72_5720-69dup
ENST00000267622.8:c.5720-72_5720-69dup MANE Select	ENSP00000267622.4:n.5720-72_5720-69dup
NM_001321851.1:c.5717-72_5717-69dup	NP_001308780.1:n.5717-72_5717-69dup
NM_004239.3:c.5720-72_5720-69dup	NP_004230.2:n.5720-72_5720-69dup
ENST00000554357.5:c.4866-72_4866-69dup
XM_005268214.2:c.4394-72_4394-69dup	XP_005268271.1:n.4394-72_4394-69dup
XM_005268215.2:c.2690-72_2690-69dup	XP_005268272.1:n.2690-72_2690-69dup
XM_006720321.2:c.5717-72_5717-69dup	XP_006720384.1:n.5717-72_5717-69dup
XM_017021787.2:c.5015-72_5015-69dup	XP_016877276.1:n.5015-72_5015-69dup
XM_017021788.2:c.4394-72_4394-69dup	XP_016877277.1:n.4394-72_4394-69dup